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nsv5523542

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,309

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 177 SVs from 32 studies. See in: genome view    
Submitted genomic20,029,451-20,031,759Question Mark
Overlapping variant regions from other studies: 150 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):20,140,260-20,142,568Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523542Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1920,029,45120,031,759
nsv5523542RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1920,140,26020,142,568

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722157deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722157Submitted genomicNC_000019.10:g.200
29451_20031759del
GRCh38 (hg38)NC_000019.10Chr1920,029,45120,031,759
nssv17722157RemappedPerfectNC_000019.9:g.2014
0260_20142568del
GRCh37.p13First PassNC_000019.9Chr1920,140,26020,142,568

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17722157<0.00116404
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